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ENDOSKELETON TA INTERBODY FUSION DEVICE (IBD)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080615
510(k) Type
Traditional
Applicant
Titan Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
105 days
Submission Type
Summary

ENDOSKELETON TA INTERBODY FUSION DEVICE (IBD)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080615
510(k) Type
Traditional
Applicant
Titan Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
105 days
Submission Type
Summary